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The British Journal of Dermatology|August 27, 2005
Molecular basis of hypotrichosis with juvenile macular dystrophy in two siblingsM Indelman, R Leibu, A Jammal, et al.
Clinical and Experimental Dermatology|January 25, 2005
Epidermolytic hyperkeratosis type PS-1 caused by aberrant splicing of KRT1O Tal, R Bergman, J Alcalay, et al.
Clinical and Experimental Dermatology|November 21, 2008
Novel mutations in DSG1 causing striate palmoplantar keratodermaD Hershkovitz, J Lugassy, M Indelman, et al.
The British Journal of Dermatology|March 26, 2003
Compound heterozygosity for mutations in the hairless gene causes atrichia with papular lesionsM Indelman, R Bergman, G G Lestringant, et al.
Clinical and Experimental Dermatology|May 10, 2006
A homozygous missense mutation in PEPD encoding peptidase D causes prolidase deficiency associated with hyper-IgE syndromeT Hershkovitz, G Hassoun, M Indelman, et al.
The British Journal of Dermatology|January 30, 2016
Segmental basal cell naevus syndrome caused by an activating mutation in smoothenedZ Khamaysi, R Bochner, M Indelman, et al.
Clinical and Experimental Dermatology|March 8, 2007
Novel CDH3 mutations in hypotrichosis with juvenile macular dystrophyM Indelman, J Eason, M Hummel, et al.
Clinical and Experimental Dermatology|April 30, 2013
Non-syndromic autosomal recessive congenital ichthyosis in the Israeli populationS Israeli, I Goldberg, D Fuchs-Telem, et al.
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